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Gene Gene information from NCBI Gene database.
Entrez ID 284612
Gene name Synaptophysin like 2
Gene symbol SYPL2
Synonyms (NCBI Gene)
MG29
Chromosome 1
Chromosome location 1p13.3
miRNA miRNA information provided by mirtarbase database.
110 Show/Hide all (110)
miRTarBase ID miRNA Experiments Reference
MIRT039687 hsa-miR-615-3p CLASH 23622248
MIRT1406982 hsa-miR-1185 CLIP-seq
MIRT1406983 hsa-miR-1253 CLIP-seq
MIRT1406984 hsa-miR-1303 CLIP-seq
MIRT1406985 hsa-miR-1305 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8 Show/Hide all (8)
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0006874 Process Intracellular calcium ion homeostasis IEA
GO:0007507 Process Heart development IEA
GO:0008021 Component Synaptic vesicle IEA
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5VXT5
Protein name Synaptophysin-like protein 2
Protein function Involved in communication between the T-tubular and junctional sarcoplasmic reticulum (SR) membranes.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01284 MARVEL 30 → 232 Membrane-associating domain Domain
Sequence
Sequence length 272
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Reference Evidence Score
CHRONIC KIDNEY DISEASE — GWAS catalog 20383146
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (7)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Aortic Valve Stenosis Aortic Valve Sclerosis BEFREE 28687561
★★★★★
★☆☆☆☆
Found in Text Mining only
Congestive heart failure Congestive Heart Failure BEFREE 28706255
★★★★★
★☆☆☆☆
Found in Text Mining only
Heart failure Heart Failure BEFREE 28706255
★★★★★
★☆☆☆☆
Found in Text Mining only
Obesity Obesity Pubtator 25406998 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Obesity Morbid Obesity Pubtator 25406998 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Obesity, Morbid Obesity BEFREE 25406998
★★★★★
★☆☆☆☆
Found in Text Mining only
Senile Plaques Senile Plaques BEFREE 22290180
★★★★★
★☆☆☆☆
Found in Text Mining only